# Nuclemed S.A.

- Location (FDA's records): Hudson, NH
- FDA decisions: 2 (2009–2009): 2 510(k) clearances
- Product codes: MUJ (1), HAW (1)
- Predicates its devices cite: 11 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Computerized Medical Systems, Inc.: 3 (https://510kreport.com/company/computerized-medical-systems)
- Adac Laboratories: 2 (https://510kreport.com/company/adac-laboratories)
- Lifeline Software, Inc.: 1 (https://510kreport.com/company/lifeline-software)
- D3 Radiation Planning: 1 (https://510kreport.com/company/d3-radiation-planning)
- Nucletron Corp.: 1 (https://510kreport.com/company/nucletron)
- Prodigm, Inc.: 1 (https://510kreport.com/company/prodigm)
- 3D Line Medical Systems S.R.L.: 1 (https://510kreport.com/company/3d-line-medical-systems)
- Elekta Instrument AB: 1 (https://510kreport.com/company/elekta-instrument)

## Recent decisions
- K090190: Win-Neus Stereotactic Surgery Treatment Planning System (Oct 9, 2009)
- K090182: Module Integrated Radiotherapy System (Mirs) (May 4, 2009)

Source page: https://510kreport.com/company/nuclemed